Canonical Allele Identifier: PA645385980
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 373281
ClinVar RCV Id: RCV000412883
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Ala337Val
CA16042835
NM_001909.5:c.1010C>T